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Sweden· SE-20131130000029

Xydalba 500 mg Pulver till koncentrat till infusionsvätska, lösning

A medicinal product containing dalbavancin, registered in Sweden by AbbVie Deutschland GmbH & Co KG.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedXydalba 500 mg Pulver till koncentrat…ATC—REGISTER NO.SE-20131130000029PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Dalbavancin
Manufacturer
AbbVie Deutschland GmbH & Co KG
Country
Sweden (SE)
ATC code
—
Reimbursed
Not published by this register
Source register
Swedish Medical Products Agency (Sweden)
Last checked
October 1, 2026

Packs & prices · 1

  • se_varunummer
    20131130000029

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Dalbavancin in 11 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All dalbavancin products

Authorised across Europe · EMA

The same active substance is authorised in 16 EEA countries. Names it is sold under:

  • Austria · Dalbavancin, Dalbavancin Accord
  • Germany · Dalbavancin Accord, Dalbavancin Baxter
  • Denmark · Dalbavancin Adalvo, Dalbavancin Teva
  • Spain · Dalbavancin Dr. Reddys, Dalbavancina Accord
  • Finland · Dalbavancin Adalvo, Dalbavancin Tillomed
  • France · Dalbavancine Accord, Dalbavancine Reddy Pharma
  • United Kingdom (Northern Ireland) · Dalbavancin Accord, Dalbavancin Reig Jofre Uk
  • Greece · Bavalda, Dalbavancin Accord
  • Iceland · Xydalba
  • Italy · Dalbavancina Accord, Dalbavancina Dr. Reddy’s
  • Liechtenstein · Xydalba
  • Malta · Bavalda, Dalbavancin Adalvo
  • Norway · Dalbavancin Tillomed, Xydalba
  • Poland · Dalbavancin Accord, Dalbavancin Reig Jofre
  • Portugal · Dalbavancina Anfarm
  • Slovakia · Dalbavancin Adalvo

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Swedish Medical Products Agency (Sweden). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/b25006e5-5946-40f5-a7d7-1c65ef4e4f37
GET /v1/drugs/b25006e5-5946-40f5-a7d7-1c65ef4e4f37?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "source": "lakemedelsverket",
  "doc_types": [
    "EPAR",
    "EMA"
  ],
  "se_npl_id": "20131130000029",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20131130000029",
  "product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/xydalba-epar-product-information_sv.pdf"
}

See everything about dalbavancin.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.